Beards S C, Robertson L J, Jackson A, Lipman J
Baragwanath Intensive Care Unit, University of Witwatersrand, Soweto, South Africa.
Postgrad Med J. 1994 Jul;70(825):499-502. doi: 10.1136/pgmj.70.825.499.
Brainstem gliomas are rare primary brain tumours which most commonly occur in the midbrain and pons. Malignant gliomas and tumours at the cervico-medullary junction are particularly unusual. The diagnosis of tumours at this site is particularly difficult using computed tomographic (CT) scanning owing to artifacts around the base of the skull. Intrinsic tumours of the cervico-medullary junction may lead to a dissociated motor deficit and the onset of symptoms can be rapid. We describe a patient in whom an isolated ascending motor deficit in association with a raised cerebrospinal fluid protein and a normal CT scan led to an erroneous diagnosis of Guillain-Barré syndrome. The patient was treated on the intensive care unit for an 8-week period before further investigation demonstrated a malignant glioma of the cervico-medullary junction. We recommend confirmation of the diagnosis of polyradiculopathy by nerve conduction studies wherever possible.
脑干胶质瘤是罕见的原发性脑肿瘤,最常发生于中脑和脑桥。恶性胶质瘤以及延髓颈髓交界处的肿瘤尤为少见。由于颅底周围的伪影,使用计算机断层扫描(CT)对该部位肿瘤进行诊断特别困难。延髓颈髓交界处的原发性肿瘤可能导致分离性运动障碍,且症状起病迅速。我们描述了一名患者,其孤立性上行性运动障碍伴脑脊液蛋白升高而CT扫描正常,导致被误诊为吉兰 - 巴雷综合征。该患者在重症监护病房接受了8周的治疗,之后进一步检查发现是延髓颈髓交界处的恶性胶质瘤。我们建议尽可能通过神经传导研究来确诊多发性神经根病。